20 and older, any sex, with Hiv or HIV Testing. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
HIV Testing Related Knowledge and PracticePrimary· pre-test(Baseline) and post-test (week 4)
A self-development scale, known as the "HIV Testing-Related Knowledge and Practice Scale," is employed to assess individuals' knowledge and practices pertaining to HIV testing. The scale consists of twenty-eight questions, encompassing both True-False and multiple-choice formats. Participants earn one point for each correct answer, contributing to a total score that ranges from the minimum scores of 0 to the maximum scores of 28. Higher scores signify a more positive outcome, indicating enhanced HIV testing-related knowledge and practice among the participants.
pre-test
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
17.17
± 1.88
Get a Learning Material Only
17.22
± 2.14
post-test
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
19.44
± 2.21
Get a Learning Material Only
17.36
± 2.69
HIV Related StigmaPrimary· pre-test (Baseline) and post-test (Week 4)
The Healthcare Provider HIV/AIDS Stigma Scale (HPASS) will be used to assess this outcome. The instrument contains 30 items, each scored on a six-point Likert scale, yielding a minimum total score of 30 and a maximum of 180. Higher scores reflect greater levels of stigma toward people living with HIV, indicating a worse outcome. Validation of the HPASS through factor analysis identified three underlying dimensions. The stereotyping dimension (11 items; score range: 11-66) reflects negative cognitions and beliefs about people living with HIV. The prejudice dimension (13 items; score range: 13-7
(pre-test)HPASS in total
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
89.39
± 16.14
Get a Learning Material Only
86.75
± 22.06
(post-test)HPASS in total
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
85.94
± 20.10
Get a Learning Material Only
88.03
± 20.44
(pre-test)stereotyping
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
36.36
± 6.85
Get a Learning Material Only
38.36
± 8.43
(post-test)stereotyping
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
36.31
± 7.66
Get a Learning Material Only
38.03
± 9.20
(pre-test)prejudice
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
35.78
± 8.51
Get a Learning Material Only
34.44
± 12.11
(post-test)prejudice
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
33.14
± 10.73
Get a Learning Material Only
34.72
± 10.31
(pre-test)discrimination
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
17.25
± 5.61
Get a Learning Material Only
13.94
± 5.68
(post-test)discrimination
Group
Value
95% CI
Get a Learning Material and a Experiential HIV Testing
16.50
± 5.59
Get a Learning Material Only
15.28
± 5.32
Sponsor's own description
This is a randomized controlled trial design. The investigators plan to recruit about 60 to 70 emergency department nurses from a medical center in Taipei, Taiwan. After completing the paper consent form, these nurses will be randomly assigned to 2 groups, which are a control group and an experimental group. The pre-test includes the demographic data sheet, HIV testing related knowledge and practice scale, and The Health Care Provider HIV/ AIDS Stigma Scale (HPASS). All nurses will receive a learning material when they finish the pre-test. In addition, the experimental group will be provided a real HIV testing and counselling by a researcher. The post-test will be finished one month later of pre-test in the control group, and one month later while the intervention completed in the experimental group. The semi-structural interview will be performed to the experimental group to collect and analyze their opinion toward the experiential HIV testing.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by National Taiwan University
Last refreshed: 1 October 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05615935.